tert-butyl3-amino-4-(hydroxymethyl)-3-(isothiazol-5-yl)pyrrolidine-1-carboxylate

Base Information

Chemical Name:tert-butyl3-amino-4-(hydroxymethyl)-3-(isothiazol-5-yl)pyrrolidine-1-carboxylate
CAS No.:1463484-93-6
Molecular Formula:C₁₃H₂₁N₃O₃S
Molecular Weight:299.394
Hs Code.:
Mol file:1463484-93-6.mol

Synonyms:tert-butyl 3-amino-4-(hydroxymethyl)-3-isothiazol-5-yl-pyrrolidine-1-carboxylate

Suppliers and Price of tert-butyl3-amino-4-(hydroxymethyl)-3-(isothiazol-5-yl)pyrrolidine-1-carboxylate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Total 2 raw suppliers

Chemical Property of tert-butyl3-amino-4-(hydroxymethyl)-3-(isothiazol-5-yl)pyrrolidine-1-carboxylate

Chemical Property:

Boiling Point:383.0±42.0 °C(Predicted)
PKA:14.93±0.10(Predicted)
Density:1?+-.0.06 g/cm3(Predicted)

Purity/Quality:: 99% ^*data from raw suppliers

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Technology Process of tert-butyl3-amino-4-(hydroxymethyl)-3-(isothiazol-5-yl)pyrrolidine-1-carboxylate

There total 6 articles about tert-butyl3-amino-4-(hydroxymethyl)-3-(isothiazol-5-yl)pyrrolidine-1-carboxylate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 65.1%

: 1463484-63-0
tert-butyl 6a-isothiazol-5-yl-3,3a,4,6-tetrahydro-1H-pyrrolo[3,4-c]isoxazole-5-carboxylate

: 1463484-93-6
tert-butyl 3-amino-4-(hydroxymethyl)-3-isothiazol-5-yl-pyrrolidine-1-carboxylate

Guidance literature:: With acetic acid; zinc; at 40 ℃; for 8h;

Reference yield:

: 145618-68-4
2-(allyl(tert-butoxycarbonyl)amino)acetic acid

: 1463484-93-6
tert-butyl 3-amino-4-(hydroxymethyl)-3-isothiazol-5-yl-pyrrolidine-1-carboxylate

Guidance literature:: Multi-step reaction with 5 steps

1.1: triethylamine / tetrahydrofuran / 3 h / 0 - 20 °C

1.2: 3 h / 0 - 20 °C

2.1: lithium diisopropyl amide / tetrahydrofuran / 0.5 h / -78 °C

2.2: 1.25 h / -78 - 20 °C

3.1: N-ethyl-N,N-diisopropylamine; titanium(IV) tetraethanolate / toluene / 2 h / 100 °C / Inert atmosphere

4.1: acetyl chloride; isopropyl alcohol / 1 h / 45 °C

4.2: 1 h / 70 °C

4.3: 1 h / 10 - 25 °C

5.1: zinc; acetic acid / 8 h / 40 °C

With titanium(IV) tetraethanolate; acetic acid; triethylamine; N-ethyl-N,N-diisopropylamine; acetyl chloride; isopropyl alcohol; zinc; lithium diisopropyl amide; In tetrahydrofuran; toluene;

Reference yield:

: 1429646-79-6
tert-butyl N-allyl-N-[2-(methoxy(methyl)amino)-2-oxo-ethyl]carbamate

: 1463484-93-6
tert-butyl 3-amino-4-(hydroxymethyl)-3-isothiazol-5-yl-pyrrolidine-1-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1.1: lithium diisopropyl amide / tetrahydrofuran / 0.5 h / -78 °C

1.2: 1.25 h / -78 - 20 °C

2.1: N-ethyl-N,N-diisopropylamine; titanium(IV) tetraethanolate / toluene / 2 h / 100 °C / Inert atmosphere

3.1: acetyl chloride; isopropyl alcohol / 1 h / 45 °C

3.2: 1 h / 70 °C

3.3: 1 h / 10 - 25 °C

4.1: zinc; acetic acid / 8 h / 40 °C

With titanium(IV) tetraethanolate; acetic acid; N-ethyl-N,N-diisopropylamine; acetyl chloride; isopropyl alcohol; zinc; lithium diisopropyl amide; In tetrahydrofuran; toluene;