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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256077Generated: October 30, 2026

HCID 13854085, compound → t-Butyl alpha-[6-(1-benzyloxycarbonyl-3-phenylpropylamino)-2-(2-furyl)-5-oxoperhydro-1,4-thiazepin-4-yl]acetate

https://huagongshe.com/reaction/256077

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 13854085HCID 13854085—
ReactantBenzyl 2-bromo-4-phenylbutyrateHCID 19024556—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Productt-Butyl alpha-[6-(1-benzyloxycarbonyl-3-phenylpropylamino)-2-(2-furyl)-5-oxoperhydro-1,4-thiazepin-4-yl]acetateHCID 20164970—

Reaction Steps

Following the procedure described in Example 42(h), 0.30 g of t-butyl α-[6-amino-2-(2-furyl)-5-oxoperhydro-1,4-thiazepin-4-yl]acetate [obtained as described in Example 56(f)] was N-alkylated using 0.60 g of benzyl 2-bromo-4-phenylbutyrate. The resulting product was subjected to silica gel column chromatography, using a 1:40 by volume mixture of ethyl acetate and methylene chloride as eluent, to separate it into two isomers, A and B, (ascribed to the asymmetric carbon atom to which the phenethyl group is attached).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04699905
Source datasetuspto-grants-1987_10
ORD IDord-55e3d8846b8f4879b891719ab34d3d66
Source noteuspto-grants-1987_10