acetic acid 7-acetoxy-6-benzyloxy-3a,4,6,7,7a,8-hexahydro-3H,5H-2-oxa-1,4a-diaza-s-indacen-8-yl ester

Base Information

Chemical Name:acetic acid 7-acetoxy-6-benzyloxy-3a,4,6,7,7a,8-hexahydro-3H,5H-2-oxa-1,4a-diaza-s-indacen-8-yl ester
CAS No.:876175-70-1
Molecular Formula:C₂₀H₂₄N₂O₆
Molecular Weight:388.42
Hs Code.:

acetic acid 7-acetoxy-6-benzyloxy-3a,4,6,7,7a,8-hexahydro-3<i>H</i>,5<i>H</i>-2-oxa-1,4a-diaza-<i>s</i>-indacen-8-yl ester

Synonyms:acetic acid 7-acetoxy-6-benzyloxy-3a,4,6,7,7a,8-hexahydro-3H,5H-2-oxa-1,4a-diaza-s-indacen-8-yl ester

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Chemical Property of acetic acid 7-acetoxy-6-benzyloxy-3a,4,6,7,7a,8-hexahydro-3H,5H-2-oxa-1,4a-diaza-s-indacen-8-yl ester

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Technology Process of acetic acid 7-acetoxy-6-benzyloxy-3a,4,6,7,7a,8-hexahydro-3H,5H-2-oxa-1,4a-diaza-s-indacen-8-yl ester

There total 9 articles about acetic acid 7-acetoxy-6-benzyloxy-3a,4,6,7,7a,8-hexahydro-3H,5H-2-oxa-1,4a-diaza-s-indacen-8-yl ester 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: 81.0%

: 876175-69-8
Acetic acid (2R,3S,4R)-2-((R)-1-acetoxy-2-hydroxyimino-ethyl)-1-allyl-4-benzyloxy-pyrrolidin-3-yl ester

: 876175-70-1
acetic acid 7-acetoxy-6-benzyloxy-3a,4,6,7,7a,8-hexahydro-3H,5H-2-oxa-1,4a-diaza-s-indacen-8-yl ester

Guidance literature:: With dmap; N-chloro-succinimide; In dichloromethane; at 25 ℃; for 48h;
DOI:10.1021/ol052716a

Reference yield:

: 876175-57-4
(3aR,4aS,5R,7aS,7bR)-7-Allyl-2,2-dimethyl-hexahydro-[1,3]dioxolo[4',5':4,5]furo[3,2-b]pyrrol-5-ol

: 876175-70-1
acetic acid 7-acetoxy-6-benzyloxy-3a,4,6,7,7a,8-hexahydro-3H,5H-2-oxa-1,4a-diaza-s-indacen-8-yl ester

Guidance literature:: Multi-step reaction with 7 steps

1: 92 percent / NaH / tetrahydrofuran / 0.1 h / Heating

2: 97 percent / H₂SO₄ / acetonitrile / 48 h / 25 °C

3: hydrochloric acid / 18 h / 0 °C

4: 910 mg / pyridine; DMAP / 12 h / 25 °C

5: HgO; HgCl₂ / H₂O; acetone / 1.5 h / Heating

6: 95 mg / pyridine; NH₂OH*HCl / ethanol / 5 h / 25 °C

7: 81 percent / N-chlorosuccinimide; DMAP / CH₂Cl₂ / 48 h / 25 °C

With pyridine; hydrogenchloride; dmap; N-chloro-succinimide; sulfuric acid; hydroxylamine hydrochloride; sodium hydride; mercury dichloride; mercury(II) oxide; In tetrahydrofuran; ethanol; dichloromethane; water; acetone; acetonitrile;
DOI:10.1021/ol052716a

Reference yield:

: 876175-59-6
(3R,3aR,6R,6aS)-4-Allyl-6-benzyloxy-hexahydro-furo[3,2-b]pyrrole-2,3-diol

: 876175-70-1
acetic acid 7-acetoxy-6-benzyloxy-3a,4,6,7,7a,8-hexahydro-3H,5H-2-oxa-1,4a-diaza-s-indacen-8-yl ester

Guidance literature:: Multi-step reaction with 5 steps

1: hydrochloric acid / 18 h / 0 °C

2: 910 mg / pyridine; DMAP / 12 h / 25 °C

3: HgO; HgCl₂ / H₂O; acetone / 1.5 h / Heating

4: 95 mg / pyridine; NH₂OH*HCl / ethanol / 5 h / 25 °C

5: 81 percent / N-chlorosuccinimide; DMAP / CH₂Cl₂ / 48 h / 25 °C

With pyridine; hydrogenchloride; dmap; N-chloro-succinimide; hydroxylamine hydrochloride; mercury dichloride; mercury(II) oxide; In ethanol; dichloromethane; water; acetone;
DOI:10.1021/ol052716a