benzyl N-<2-<<1,1-dimethyl-2--2-oxoethyl>amino>-2-thioxoethyl>carbamate

Base Information

• Chemical Name: benzyl N-<2-<<1,1-dimethyl-2--2-oxoethyl>amino>-2-thioxoethyl>carbamate
• CAS No.: 238748-87-3
• Molecular Formula: C₂₁H₂₅N₃O₃S
• Molecular Weight: 399.514
• Mol file: 238748-87-3.mol

Synonyms:benzyl N-<2-<<1,1-dimethyl-2--2-oxoethyl>amino>-2-thioxoethyl>carbamate

Chemical Property of benzyl N-<2-<<1,1-dimethyl-2--2-oxoethyl>amino>-2-thioxoethyl>carbamate

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of benzyl N-<2-<<1,1-dimethyl-2--2-oxoethyl>amino>-2-thioxoethyl>carbamate

There total 3 articles about benzyl N-<2-<<1,1-dimethyl-2--2-oxoethyl>amino>-2-thioxoethyl>carbamate 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:

2-(((benzyloxy)carbonyl)amino)ethanethioic S-acid (16707-70-3) → benzyl N-<2-<<1,1-dimethyl-2--2-oxoethyl>amino>-2-thioxoethyl>carbamate (238748-87-3)

Guidance literature:

Multi-step reaction with 2 steps

1: CH₂Cl₂ / 1 h / Ambient temperature

2: 1.) ZnCl₂, 2.) HCl / 1.) AcOH, rt, 30 min, 2.) AcOH, rt, 15 min

With hydrogenchloride; zinc(II) chloride; In dichloromethane;

DOI:10.1002/(SICI)1522-2675(19990609)82:6<888::AID-HLCA888>3.0.CO;2-5

Reference yield:

N-(Benzyloxycarbonyl)glycine (1138-80-3) → benzyl N-<2-<<1,1-dimethyl-2--2-oxoethyl>amino>-2-thioxoethyl>carbamate (238748-87-3)

Guidance literature:

Multi-step reaction with 3 steps

1: 1.) isobutyl chloroformate, N-methylmorpholine, 2.) H₂S / 1.) THF, -10 deg C, 5 min, 2.) THF, -10 deg C, 1 h

2: CH₂Cl₂ / 1 h / Ambient temperature

3: 1.) ZnCl₂, 2.) HCl / 1.) AcOH, rt, 30 min, 2.) AcOH, rt, 15 min

With 4-methyl-morpholine; hydrogenchloride; hydrogen sulfide; zinc(II) chloride; isobutyl chloroformate; In dichloromethane;

DOI:10.1002/(SICI)1522-2675(19990609)82:6<888::AID-HLCA888>3.0.CO;2-5

Reference yield:

benzyl N-<2-<<1,1-dimethyl-2--2-thioxoethyl>amino>-2-oxoethyl>carbamate (238748-85-1) → benzyl N-<2-<<1,1-dimethyl-2--2-oxoethyl>amino>-2-thioxoethyl>carbamate (238748-87-3)

Guidance literature:

With hydrogenchloride; zinc(II) chloride; Yield given; Multistep reaction; 1.) AcOH, rt, 30 min, 2.) AcOH, rt, 15 min;

DOI:10.1002/(SICI)1522-2675(19990609)82:6<888::AID-HLCA888>3.0.CO;2-5

upstream raw materials:

benzyl N-<2-<<1,1-dimethyl-2--2-thioxoethyl>amino>-2-oxoethyl>carbamate

2-(((benzyloxy)carbonyl)amino)ethanethioic S-acid

N-(Benzyloxycarbonyl)glycine

Downstream raw materials:

benzyl N-[1-(4,5-dihydro-4,4-dimethyl-5-oxo-1,3-thiazol-2-yl)methyl]carbamate

methyl (2S,3S)-2-[2-({[(benzyloxy)carbonyl]amino}ethanethioamido)-2-methylpropanamido]-3-methylpentanoate

(2S,3S)-2-[2-({[(benzyloxy)carbonyl]amino}ethanethioamido)-2-methylpropanamido]-3-methylpentanoic acid